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Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects.
Abolhassani H, Vitali M, Lougaris V, Giliani S, Parvaneh N, Parvaneh L, Mirminachi B, Cheraghi T, Khazaei H, Mahdaviani SA, Kiaei F, Tavakolinia N, Mohammadi J, Negahdari B, Rezaei N, Hammarstrom L, Plebani A, Aghamohammadi A. Abolhassani H, et al. Among authors: parvaneh l, parvaneh n. Expert Rev Clin Immunol. 2016;12(4):479-86. doi: 10.1586/1744666X.2016.1139451. Epub 2016 Feb 24. Expert Rev Clin Immunol. 2016. PMID: 26910880
Clinical, immunological and molecular characteristics of 37 Iranian patients with X-linked agammaglobulinemia.
Aghamohammadi A, Fiorini M, Moin M, Parvaneh N, Teimourian S, Yeganeh M, Goffi F, Kanegane H, Amirzargar AA, Pourpak Z, Rezaei N, Salavati A, Pouladi N, Abdollahzade S, Notarangelo LD, Miyawaki T, Plebani A. Aghamohammadi A, et al. Among authors: parvaneh n. Int Arch Allergy Immunol. 2006;141(4):408-14. doi: 10.1159/000095469. Epub 2006 Aug 30. Int Arch Allergy Immunol. 2006. PMID: 16943681
Mortality and morbidity in common variable immunodeficiency.
Aghamohammadi A, Pouladi N, Parvaneh N, Yeganeh M, Movahedi M, Gharagolou M, Pourpak Z, Rezaei N, Salavati A, Abdollahzade S, Moin M. Aghamohammadi A, et al. Among authors: parvaneh n. J Trop Pediatr. 2007 Feb;53(1):32-8. doi: 10.1093/tropej/fml077. Epub 2006 Dec 13. J Trop Pediatr. 2007. PMID: 17166933
Gastrointestinal manifestations in patients with common variable immunodeficiency.
Khodadad A, Aghamohammadi A, Parvaneh N, Rezaei N, Mahjoob F, Bashashati M, Movahedi M, Fazlollahi MR, Zandieh F, Roohi Z, Abdollahzade S, Salavati A, Kouhi A, Talebpour B, Daryani NE. Khodadad A, et al. Among authors: parvaneh n. Dig Dis Sci. 2007 Nov;52(11):2977-83. doi: 10.1007/s10620-006-9736-6. Epub 2007 Apr 12. Dig Dis Sci. 2007. PMID: 17431775
171 results